The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
117130223 11713022 3 F 20080807 20160621 20151108 20160703 EXP ZW-BRISTOL-MYERS SQUIBB COMPANY-14902563 BRISTOL MYERS SQUIBB 36.00 YR F Y 0.00000 20160703 OT ZW ZW

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
117130223 11713022 1 PS EFAVIRENZ EFAVIRENZ 1 Oral 600 MG, QD 20972 600 MG QD
117130223 11713022 2 SS VIDEX DIDANOSINE 1 Oral 400 MG, QD 0 400 MG QD
117130223 11713022 3 SS VIDEX DIDANOSINE 1 Oral 250 MG, QD 0 250 MG QD
117130223 11713022 4 SS ALUVIA LOPINAVIRRITONAVIR 1 Oral 1500 MG, QD 0 1500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117130223 11713022 1 Antiretroviral therapy
117130223 11713022 2 Antiretroviral therapy
117130223 11713022 4 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
117130223 11713022 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117130223 11713022 Abortion spontaneous
117130223 11713022 Maternal exposure during pregnancy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
117130223 11713022 1 20041228 0
117130223 11713022 2 20050616 0
117130223 11713022 3 20080612 0
117130223 11713022 4 20071101 0